p27(kip1) functional regulation in human cancer: a potential target for therapeutic designs.

Abstract

The mitotic cell cycle is a tightly regulated process that ensures the correct division of one cell into two daughter cells. Progress along the different phases of the cell cycle is positively regulated by the sequential activation of a family of serine-threonine kinases called CDKs (Cyclin Dependent Kinases). Their activity is counteracted by small proteins known as CDK inhibitors (CKI) that ensure the correct timing of CDK activation in the different phases of the cell cycle. The present review will deal with the role of one of this CKI, p27(kip1), in human cancer, focusing in particular on the mechanisms underlying its functional inactivation in tumor cells. p27(kip1) protein downregulation is usually achieved by proteasomal degradation and is often correlated to a worse prognosis in several types of human cancers, resulting in the reduction of disease free and overall survival. More recently, it has been proposed that p27(kip1) protein, rather than degraded, can be functionally inactivated. The mechanisms and the implications of these two types of p27(kip1) deregulation will be discussed and some potential therapeutic approaches targeting p27(kip1) functions will be proposed.

• Authors: B Belletti, M S Nicoloso, M Schiappacassi, E Chimienti, S Berton, F Lovat, A Colombatti, G Baldassarre
• Journal: Current medicinal chemistry (Curr Med Chem) Vol. 12 Issue 14 Pg. 1589-605 ( 2005) ISSN: 0929-8673 [Print] United Arab Emirates
• PMID: 16022660 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Cell Cycle Proteins
• Tumor Suppressor Proteins
• Cyclin-Dependent Kinase Inhibitor p27
• Cyclin-Dependent Kinases

Topics

• Animals
• Cell Cycle (physiology)
• Cell Cycle Proteins (antagonists & inhibitors, genetics, metabolism, physiology)
• Cell Division (physiology)
• Cyclin-Dependent Kinase Inhibitor p27
• Cyclin-Dependent Kinases (antagonists & inhibitors, metabolism)
• Gene Expression Regulation, Neoplastic
• Gene Silencing
• Genetic Therapy (methods)
• Humans
• Neoplasms (drug therapy, metabolism, pathology)
• Tumor Suppressor Proteins (antagonists & inhibitors, genetics, metabolism, physiology)